Prazosin Hydrochloride
- Product NDC
- 70518-2177
- 11-digit product format
- 705182177
- Labeler code
- 70518
- Product ID
- 70518-2177_dae5789b-bb08-ca3e-e053-2a95a90a6cb4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prazosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA210971
- Marketing category
- ANDA
- Marketing start
- 2019-07-01
- Marketing end
- 0000-00-00
- Substance
- PRAZOSIN HYDROCHLORIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2177 | PRAZOSIN HYDROCHLORIDE CAPSULE [REMEDYREPACK INC.] | 9 | Legacy NDC | 20250308_f82d47a4-d1ab-454b-a92d-3bab12ee4abf.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2177-0 | 70518217700 | 30 CAPSULE in 1 BLISTER PACK (70518-2177-0) | 30 capsule | 2019-07-01 | 0000-00-00 | No | No | Current |
| 70518-2177-1 | 70518217701 | 30 CAPSULE in 1 BLISTER PACK (70518-2177-1) | 30 capsule | 2020-05-28 | 0000-00-00 | No | No | Current |